Our research focuses on the application of computational methods to the study of organic reactivity in diverse environments (in the gas phase, in solution, in the interiors of biological macromolecules, on metal surfaces, as part of organometallic complexes). The intimate relationship between theory and experiment pervades each of these endeavors, and a focus of our work is the design of molecular architectures with unusual reactivity.

 

"Playfulness is an incentive for the scientist and a motor of progress."

- Rolf Huisgen, The Adventure Playground of Mechanisms and Novel Reactions, 1994.

 

Reaction Design and Theories of Reactivity

 

 

Reactive Intermediate Promoted Polycyclization (RIPP) Reactions

Hiscotropic Rearrangements

A New Outlook on Pericyclic Reactions

 

Theoretical Bioorganic and Bioinorganic Chemistry

 

 

Complexity Creation in Bio- and Biomimetic Syntheses of Natural Products

Theozymes

Nonclassical Cations in Biology

Terpenoid Biosynthesis

Ladderane Lipids

Enzyme Inhibitor Design

Noncovalent Catalysis of Biological Decarboxylations

Antibody Catalyzed Organic Reactions

Biosynthesis and Molecular Pharmacology of Nitric Oxide and Nitroxyl

 

Organic Molecules with Unusual Properties

 

 

5-Center 4-Electron Cations and Their Relatives

Sigmatropic Shiftamers

Sigma-Polyacenes

Fickle Hexadienes

Tetrathiafulvalenes under Extreme Conditions

 

Physical Organometallic Chemistry

 

 

Metal-Promoted Sigmatropic Shifts

Iron-Promoted Electrocyclic Reactions

Interactions of Chromium Arenes with Reactive Intermediates

 

Rates, Regio- and Stereoselectivity of Synthetically Useful Reactions

 

 

Semibullvalene Bromination

The Cationic Cascade Route to Longifolene

Rearrangements of Housane Radical Cations

Stereoselectivity of Intramolecular Diels-Alder Reactions

Regio- and Stereoselectivity of alpha-Lactam Ring-Opening Reactions

 

 

 

"...it is through training in pure research that the mind is best prepared to capitalize broadly on chances as they arise... My area, physical organic chemistry, is a highly interdisciplinary pursuit that provides the principles for the design and synthesis of organic molecules with the goal of uncovering the origins of their structure and properties. It is the conceptual basis for the modern arenas of stereoselective, biomimetic, and materials chemistry. It provides basic tools for medicinal, environmental, and biological chemistry. So, why is physical organic chemistry viewed as off-limits to young scientists who have hopes of establishing research funding? What spoiled the passion for such a central theme in chemistry? Could it be that 'visionaries' who 'knew the way' were allowed to project their futures on that of the field without regard for diversity?"

- Jay Siegel, C&EN, March 26, 2001, p.114

 

 

"..the compounds just described [(C5H5)2MX2, M = V, Nb, Ta, X = Cl, Br] were the lineal ancestors of today's marvelous so-called single-site catalysts for olefin polymerization. They were discovered, I would like to emphasize, not by people who had written a grant proposal to work on olefin polymerization, but by people who were funded to do fundamental research that had no predictable practical use."

- F. A. Cotton, J. Organomet. Chem. 2001, 637-639, 18-26

 

 

"It has always seemed to me that the most attractive applications of theory are to explore the unknown. If you want to find something truly new, your chances are better if you look in new places."

- Paul Schleyer, J. Comp. Chem. 2001, 13, ix-xi